Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

17 matching diseasesClear search ×

Intermediate maple syrup urine disease

Intermediate BCKD deficiency · Intermediate MSUD

ORPHA:268162

Classic maple syrup urine disease

Classic BCKD deficiency · Classic MSUD

ORPHA:268145

Combined immunodeficiency due to ITK deficiency

ITK deficiency · Autosomal recessive lymphoproliferative disease due to ITK deficiency

ORPHA:538963

Growth delay due to insulin-like growth factor type 1 deficiency

Growth delay-hearing loss-intellectual disability syndrome · IGF-1 deficiency

ORPHA:73272

Intermediate Charcot-Marie-Tooth disease

Intermediate CMT · Intermediate hereditary motor and sensory neuropathy

ORPHA:476123

Intermediate collagen VI-related muscular dystrophy

Intermediate COL6-RD

ORPHA:646113

Intermediate DEND syndrome

Developmental delay-epilepsy-neonatal diabetes syndrome, intermediate form

ORPHA:99989

Intermediate uveitis

IU

ORPHA:279914

Intermittent maple syrup urine disease

Intermittent BCKD deficiency · Intermittent MSUD

ORPHA:268173

Maple syrup urine disease

BCKD deficiency · BCKDH deficiency

ORPHA:511

Multiple mitochondrial dysfunctions syndrome type 2

BOLA3 deficiency · MMDS2

ORPHA:401874

Multiple mitochondrial dysfunctions syndrome type 3

IBA57 deficiency · MMDS3

ORPHA:363424

Multiple mitochondrial dysfunctions syndrome type 5

ISCA1 deficiency · MMDS5

ORPHA:569274

NAD(P)HX dehydratase deficiency

CARKD deficiency

ORPHA:555402

Neonatal adrenoleukodystrophy

NALD · Intermediate peroxisome biogenesis disorder-Zellweger spectrum disorder

ORPHA:44

Progressive familial intrahepatic cholestasis type 2

BSEP deficiency · PFIC2

ORPHA:79304

X-linked agammaglobulinemia

BTK-deficiency · Bruton type agammaglobulinemia

ORPHA:47